Inflammation and Coronary Artery Disease: Role of AT1-Receptor Antagonism

NCT ID: NCT00274144

Last Updated: 2013-11-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

42 participants

Study Classification

INTERVENTIONAL

Study Start Date

2001-12-31

Study Completion Date

2004-05-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Effects of AT1 receptor antagonist telmisartan on the primary endpoint inflammatory parameters in patients with coronary artery disease (CAD). Secondary endpoints are alterations in clinical course and blood pressure

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Methodology:

Randomised, double-blind and placebo-controlled parallel group design

Planned/actual number of subjects:

Enrolled: 40/50 randomised: 40/42 completed: 40/42

Diagnosis and main criteria for inclusion:

Treated essential hypertension with a mean seated DBP/SBP smaller than 95 mmHg/160 mmHg, coronary artery disease confirmed by catheterization and age equal or greater than 18 years of age.

Duration of treatment:

12 weeks: telmisartan 40 mg or placebo 40 mg

Study Hypothesis:

The statistical null hypothesis is that in patients with CAD and mild-to-moderate hypertension, a 84-day therapy with 40 mg telmisartan causes changes in inflammatory and leukocyte adhesion parameters. The alternative hypothesis is that this therapy does not influence inflammatory and leukocyte adhesion parameters. This hypothesis is tested by the nonparametric Wilcoxon test for unpaired samples.

Comparison(s):

Placebo 40 mg

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Hypertension Coronary Arteriosclerosis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

telmisartan 40 mg

Intervention Type DRUG

placebo 40 mg

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Treated essential hypertension with a mean seated DBP \< 95 mm Hg and a mean seated SBP \< 160 mm Hg at the randomisation visit (baseline)
2. Coronary artery disease confirmed by cardiac catheterization
3. \> 18 years of age
4. Ability to stop current antihypertensive therapy with ACE inhibitors, angioten-sin II receptor antagonist or lipid lowering therapy with statins without risk to the patient in the run-in period of two to four weeks and during the study period.
5. Ability to provide written informed consent.

Exclusion Criteria

1. Acute coronary syndromes.
2. Acute or chronic heart failure (left ventricular ejection fraction \< 45 %).
3. Symptomatic valvular heart disease.
4. Inflammatory diseases (e.g., acute infection, rheumatic diseases, collagenosis).
5. Pre-menopausal women (last menstruation \< 1 year prior to start of run-in period) who:

* Are not surgically sterile.
* Are nursing.
* Are of child-bearing potential and are NOT practicing acceptable means of birth control, do NOT plan to continue using this method throughout the study and do NOT agree to submit to periodic pregnancy testing during participation in studies of \> 3-months duration. Acceptable methods of birth control include oral, implantable or injectable contraceptives.
6. Known or suspected secondary hypertension.
7. Mean sitting SBP \> 160 mm Hg or mean sitting DBP \> 95 mm Hg during any visit.
8. Hepatic and/or renal dysfunction as defined by the following laboratory parameters:

* SGPT(ALT) or SGOT(AST) \> than 2 times the upper limit of normal range .
* Serum creatinine \> 2.3 mg/dL.
9. Bilateral renal artery stenosis, renal artery stenosis in a solitary kidney, patients post-renal transplant or with only one kidney.
10. Clinically relevant hypokalaemia or hyperkalaemia.
11. Uncorrected volume depletion.
12. Uncorrected sodium depletion.
13. Primary aldosteronism.
14. Hereditary fructose intolerance.
15. Biliary obstructive disorders.
16. Patients who have previously experienced symptoms characteristic of angioedema during treatment with ACE inhibitors or angiotensin II receptor antagonists.
17. History of drug or alcohol dependency within 6 months.
18. Chronic administration of any medications known to affect blood pressure, except medication allowed by the protocol (cf. 4.2.1).
19. Current participation in another trial, or participation in a trial within a period of one month.
20. Known hypersensitivity to any component of the formulation.
21. Has no contra-indication to a placebo run-in period (e.g., recent stroke or MI).
22. Any other clinical condition which, in the opinion of the principal investigator, would not allow safe completion of the protocol and safe administration of telmisartan.
Minimum Eligible Age

19 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Boehringer Ingelheim

INDUSTRY

Sponsor Role lead

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Boehringer Ingelheim Study Coordinator

Role: STUDY_CHAIR

B.I. Pharma GmbH & Co. KG

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Universitätsklinik des Saarlandes

Homburg/Saar, , Germany

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Germany

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

502.385

Identifier Type: -

Identifier Source: org_study_id